Guest guest Posted January 26, 2005 Report Share Posted January 26, 2005 Mike, I also have an oncologist, for tumours that my body tends to grow, and have found that they are the best for pain control. I guess it is because of their specialty, they deal with chronically pained patients due to their cancers. My oncologist is willing to look after me for my pancreatitis spells also, which I am glad about. Probably because the last few years of it were caused by a stricture from surgery I had in 2001. He was the surgeon, but the stricture was caused by excess scar tissue my body has a tendency to make. I have no problem asking for any meds that help me better when I am under this doctor's care. (His residents are a different matter). And most times, if I ask them to ask my surgical oncologist when the residents um and arr about me having increases or other meds to help me with my nausea or side effects of the medicines, he usually tells them to go ahead. As for going to the ER, I feel that they will look and treat me badly if I start off with..I need Dilaudid, for Demerol and Morphine don't help with the pain any more. One doctor found a combination that worked for me, yet there are many doctors who don't like to accomodate that. I do carry a letter around with me now from my family doctor, stating that my condition is serious and the best pain meds for me and that i am not a drug seeker. After I got it from her, as fates would have it I haven't had the need to use it yet. Will see if it works if I do have to use it. I had one resident who didn't even want to give me benedryl to help with the itching and nausea I was experiencing. Yet another oncologist I saw before he left for another state had no qualms whatsoever with Benedryl. Better than Phenergan in my books. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 26, 2005 Report Share Posted January 26, 2005 I also have a few letters with me, one from the oncologist(sp?) and one from my family doctor whom I get the pain meds from, but since my hospitals records are all digitalized, once they look me up I have no troubles anymore. I too had a stricture in my pancreas duct, it wasn't found for a year so the tail end kinda ate itself,lol, so it got removed(over half total) with the spleen and gall bladder, surgoen called it a blue-plate special sugery, 3 for the price of one. Funny thing nobody ever figured out with me was my CP caused by the stricture, or was the stricture cause by having CP first, then what caused the CP to begin with. Its like the chicken and the egg, which came first. I'm an idiot they said, or idiopathic,lol, both could be true my wife says. Anyone else name their pancreas? Mine is Ed. Ed doesn't play well with others. Mike Quote Link to comment Share on other sites More sharing options...
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